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EMERGE MEDICAL PERIARTICULAR AND LOCKING LARGE FRAGMENT SYSTEM

K140119 Class II Traditional
Decision Date
2014-03-12
Sponsor / Applicant
Emerge Medical

Technical Specification

510(k) Submission ID K140119
Product Code HRS
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 2014-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMERGE MEDICAL PERIARTICULAR AND LOCKING LARGE FRAGMENT SYSTEM received FDA 510(k) clearance under submission number K140119, sponsored by Emerge Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2014-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code HRS and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.